| Literature DB >> 24954533 |
Dan Huang1, Shujuan Jiang1, Yuanyuan Zhang1, Xiaoliang Liu1, Jiubin Zhang2, Rong He3.
Abstract
Brachydactyly type B, an autosomal dominant disorder that is characterized by hypoplasia of the distal phalanges and nails, can be divided into brachydactyly type B1 (BDB1) and brachydactyly type B2 (BDB2). BDB1 is caused by mutations in the receptor tyrosine kinase gene ROR2, which maps to chromosome 9q22, whereas BDB2 is caused by point mutations in the bone morphogenetic protein antagonist NOGGIN. Here, we report a three-generation Chinese family with dominant inheritance of the BDB1 limb phenotype. Sequence analysis identified a novel heterozygous base deletion (c.1396-1398delAA) in the gene ROR2 in all affected family members. This new deletion is expected to produce a truncated Ror2 protein with a new polypeptide of 57 amino acids at the C-terminal.Entities:
Keywords: Brachydactyly type B1; Mutation; ROR2; c.1396–1398delAA
Mesh:
Substances:
Year: 2014 PMID: 24954533 DOI: 10.1016/j.gene.2014.06.035
Source DB: PubMed Journal: Gene ISSN: 0378-1119 Impact factor: 3.688